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作 者:侯磊[1] 张曦[1] 李大金[2] 张展[1] 贾莉婷[1] 熊平[3] 常彩虹[1] 王雪梅[1] 龚非力[3]
机构地区:[1]郑州大学第三附属医院,郑州450050 [2]复旦大学附属妇产科研究所,上海200011 [3]华中科技大学同济医学院免疫教研室,武汉430030
出 处:《中国免疫学杂志》2006年第4期315-319,共5页Chinese Journal of Immunology
基 金:河南省卫生厅专项基金资助项目(21764)
摘 要:目的:探讨人类白细胞抗原HLA-DQ-A1、DQB1、DPA1基因多态性与先兆子痫发病的关系。方法:采用序列特异性引物技术(PCRSSP)对46例先兆子痫患者和105例正常孕妇及其新生儿进行HLA-DQ-DPA1等位基因分型。结果:所有标本共检出11种HLADQA1基因表型、16种HLADQB1基因表型、6种HLADPA1基因表型。先兆子痫患者HLA-DQ-B10301基因频率高于正常孕妇,差异有显著性(Pc=0.032,RR=2.43,AR=0.30),其余各基因表型频率两组比较差异均无显著性。结论:HLADQB10301基因可能是一种先兆子痫发病的易感基因。Objective:To clarify whether there are susceptible HLA-DQ or HLA-DPB1 alleles in women with preeclampsia. Methods :The HLA-DQ and HLA-DPA1 typing were performed using sequence-specific amplification(PCR-SSP) in 46 patients and 105 healthy pregnant women and their newborns. Results:The HLA-DQB1 * 0301 alleles frequency was higher in patients with preeclampsia (30. 43% ) than in the tested group of healthy controls( 16. 19% ) (Pc = 0. 032 ,RR = 2.43, AR = 0. 30 ), the HLA-DQA1 and HLA- DPB1 alleles frequency were no signficiant difference between two groups, so did newborns. No difference was found in HLA-DQ or HLA-DPBlmaternal-fetal genetic sharing between them. Condusion: Results suggest that the presence of HLA-DQB1 * 0301 alleles may increase the risk of preeclampsia.
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